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Clinical Trial Summary

an unbalanced (2:1) randomized study comparing two methods of traumatic skin closure in an ER setting: BandGrip vs suture


Clinical Trial Description

Up to 45 subjects at up to 2 study sites who present to the ER for treatment of a skin laceration will be consented and randomized to treatment with suture or BandGrip. Subjects will be followed for 30 days post treatment to assess cosmetic quality of wound healing, evidence of adverse events related to closure method, and speed and completeness of wound closure and removal of closure devices. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03628690
Study type Interventional
Source BandGrip
Contact Dennis J Donohoe, MD
Phone 215-499-4458
Email ddonohoeconsult@gmail.com
Status Recruiting
Phase N/A
Start date July 15, 2018
Completion date February 2020

See also
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Completed NCT04617041 - Assessment of DAFILON® Suture Material for Skin Closure
Completed NCT04536493 - Comparison of 2 Application Techniques for LET Gel Used Prior to Simple Laceration Repair Phase 4
Recruiting NCT05383495 - Anxiolysis for Laceration Repair in Children Phase 3
Completed NCT03475901 - Virtual Reality for Anxiolysis During Laceration Repair in the Pediatric Emergency Room N/A